Paste-like bone cement

ABSTRACT

Paste containing at least one monomer for radical polymerization, at least one polymer that is soluble in said at least one monomer for radical polymerization, and at least one filling agent that is poorly soluble or insoluble in said at least one monomer for radical polymerization, wherein the filling agent is a particulate inorganic filling agent possessing a BET surface of at least 40 m 2 /g; kit comprising pastes A and B which, when mixed, form paste C, which pastes are useful for mechanical fixation of articular endoprostheses, for covering skull defects, for filling bone cavities, for femuroplasty, for vertebroplasty, for kyphoplasty, for the manufacture of spacers or for the production of carrier materials for local antibiotics therapy, as well as a form body produced from the pastes.

The present invention relates to a paste, a kit, the use of a paste orof a paste produced from a kit for mechanical fixation of articularendoprostheses, for covering skull defects, for filling bone cavities,for femuroplasty, for vertebroplasty, for kyphoplasty, for themanufacture of spacers or for the production of carrier materials forlocal antibiotics therapy, as well as a form body.

BACKGROUND OF THE INVENTION

Conventional polymethylmethacrylate bone cements (PMMA bone cements)have been known for decades and are based on the ground-breaking work ofSir Charnley (Charnley, J.: “Anchorage of the femoral head prosthesis ofthe shaft of the femur”; J. Bone Joint Surg. 42 (1960) 28-30). The basicstructure of PMMA bone cements has remained the same ever since. PMMAbone cements consist of a liquid monomer component and a powdercomponent. The monomer component generally contains (i) the monomer,methylmethacrylate, and (ii) an activator (e.g.N,N-dimethyl-p-toluidine) dissolved therein. The powder componentcomprises (i) one or more polymers that are made by polymerisation,preferably by suspension polymerisation, based on methylmethacrylate andco-monomers, such as styrene, methylacrylate or similar monomers, (ii) aradio-opaquer, and (iii) an initiator, (e.g. dibenzoylperoxide). Mixingthe powder component and the monomer component, the polymers of thepowder component in the methylmethacrylate swell which generates a doughthat can be shaped plastically. Simultaneously, the activator,N,N-dimethyl-p-toluidine, reacts with dibenzoylperoxide whichdisintegrates and forms radicals in the process. The radicals thusformed trigger the radical polymerisation of the methylmethacrylate.Upon advancing polymerisation of the methylmethacrylate, the viscosityof the cement dough increases until the cement dough solidifies and thusis cured.

The essential disadvantage of the previous PMMA bone cements for themedical user is that the user needs to mix the liquid monomer componentand the powder component in a mixing system or in crucibles right beforeapplying the cement. Mixing errors can easily occur in the process andadversely affect the quality of the cement. Moreover, the componentsmust be mixed rapidly. In this context, it is important to mix all ofthe cement powder and monomer component without forming lumps andprevent the introduction of air bubbles during the mixing process.Unlike manual mixing, the use of vacuum mixing systems prevents theformation of air bubbles in the cement dough to a large extent. Examplesof mixing systems are disclosed in patent specifications U.S. Pat. No.4,015,945, EP-A-0 674 888, and JP-A-2003181270. However, vacuum mixingsystems necessitate an additional vacuum pump and are thereforerelatively expensive. Moreover, depending on the type of cementconcerned, a certain waiting time is required after mixing the monomercomponent and the powder component until the cement dough is tack-freeand can be applied. Because of the large variety of errors that canoccur while mixing conventional PMMA bone cements, appropriately trainedpersonnel is required for this purpose. The corresponding training isassociated with considerable expenses. Moreover, mixing of the liquidmonomer component and the powder component is associated with exposureof the user to monomer vapours and particles released from thepowder-like cement.

Pasty polymethylmethacrylate bone cements containing a methacrylatemonomer for radical polymerisation, a polymer that is soluble in saidmethacrylate monomer, and a particulate polymer that is insoluble insaid methacrylate monomer have been described as an alternative to theconventional powder-liquid polymethylmethacrylate bone cements inunexamined German patent applications DE-A-10 2007 052 116, DE-A-10 2007050 762, and DE-A-10 2007 050 763. Paste-like polymethylmethacrylatebone cements of this type can be present as one-component systems (inthis case, the paste contains all components required for curing, inparticular an activatable radical initiator, e.g. a photoinitiator or aphotoinitiator system) or as two-component systems (in this case, thesystem comprises two pre-mixed pastes that are stable on storage and oneof which comprises a radical polymerisation initiator and the othercomprises a polymerisation activator). Referring to two-componentsystems, a distinction is made between a “symmetrical system” (in thiscase both pastes contain a particulate polymer that is insoluble in themethacrylate monomer) and “non-symmetrical systems” (in this case, onlyone of the two pastes contains a particulate polymer that is insolublein the methacrylate monomer).

As a result of the selected composition, the bone cement produced fromthe pastes described above possesses sufficiently high viscosity andcohesion in order to withstand the pressure from bleeding until it isfully cured. Owing to the advancing polymerisation, the paste is curedwhile the methacrylate monomers are consumed.

Aside from at least one monomer for radical polymerisation and at leastone polymer dissolved therein, the pasty polymethylmethacrylate bonecements disclosed in DE-A-10 2007 052 116, DE-A-10 2007 050 762, andDE-A-10 2007 050 763 contain polymer particles that are insoluble insaid monomer. Said insoluble polymer particles are a filling agent. Saidfilling agent has a significant influence on the viscosity of the cementpastes. The polymer particles are essential for the processingproperties to ensure that the cement pastes show as little restoringmotion as possible during the application phase of the shaping process.This allows the cement pastes to be moulded into any shape during theprocessing phase such as is generally known for conventionalpolymethylmethacrylate bone cements that are based on the mixing ofpolymer powder and monomer liquid.

The production of cross-linked polymer particles that are insoluble inmethacrylate monomers is relatively laborious and therefore expensive.For this reason, it is desirable to identify an alternative, inexpensiveparticulate material which, after admixture into mixtures ofmethacrylate monomers and polymers dissolved therein, yields pastes thatshow only minimal elastic resilience after shaping much likecross-linked polymer particles.

However, one problem is that the cross-linked polymer particles usedthus far also contributed to the mechanical stability of the cured pastycements. It is therefore important to identify an alternative fillingagent which not only ensures that the pastes have the requisiteprocessing properties, but also does not adversely affect the mechanicalparameters of the cured cements such that the mechanical stabilityrequirements of ISO 5833 are met.

SUMMARY

The present invention was based on the object to overcome thedisadvantages of prior art bone cement systems that are based on pastes,in particular with regard to the two-component systems described above.

In particular, the present invention was based on the object to providea bone cement paste, in particular a bone cement paste based on atwo-component system, which can be produced from less expensive startingmaterials than bone cement pastes known according to the prior art, butstill features the same processing properties as the pastes according tothe prior art.

A contribution to meeting the objects specified above is made by a pastecontaining at least one monomer for radical polymerisation, at least onepolymer that is soluble in said monomer for radical polymerisation, andat least one filling agent that is poorly soluble or insoluble in saidat least one monomer for radical polymerisation, whereby the fillingagent is a particulate inorganic filling agent with a BET surface of atleast 40 m²/g, particularly preferably of at least 200 m²/g, and mostpreferably of at least 300 m²/g.

The invention is based on finding that bone cement pastes that can beformed and shaped well can be produced through the use of particulateinorganic filling agents possessing a BET surface of at least 40 m²/g,which was a surprise considering the previously known pastypolymethylmethacrylate bone cements. It is surprising that the hithertocustomary cross-linked polymer particles that are insoluble inmethacrylate monomers can be replaced fully or partly by particulateinorganic filling agents that possess a BET surface of at least 40 m²/g.Inorganic filling agents of this type are markedly less expensive thancross-linked polymer particles and can therefore be used to economicadvantage in the production of pasty polymethylmethacrylate bonecements.

Surprisingly, it was feasible to produce cement pastes that met themechanical requirements of ISO 5833 after curing despite the use ofinorganic particles instead of cross-linked polymer particles.

It is particularly advantageous to use particulate inorganic fillingagents possessing a BET surface of at least 40 m²/g to produce pastybone cement pastes for kyphoplasty and vertebroplasty that contain ahigh radiopaquer fraction and have a processing time of at least 15minutes.

As a matter of principle, the paste according to the invention can be aone-component system of the type described above or can be obtainedthrough mixing the two pastes of a two-component system of the typedescribed above.

DETAILED DESCRIPTION

The paste according to the invention contains, as a component, at leastone monomer for radical polymerisation, whereby this is preferably amethacrylate monomer, in particular a methacrylate monomer that isliquid at a temperature of 25° C. and a pressure of 1,013 hPa.

Preferably, the monomer for radical polymerisation is not a bisphenolA-derived methacrylic acid ester.

Preferably, the methacrylate monomer is a methacrylic acid ester.Preferably, the methacrylic acid ester is a mono-functional methacrylicacid ester. Preferably, said substance is hydrophobic. The use ofhydrophobic monofunctional methacrylic acid esters allows laterincreases in bone cement volume due to the uptake of water and thusdamage to the bone to be prevented. According to a preferred embodiment,the monofunctional methacrylic acid ester is hydrophobic if it containsno further polar groups aside from the ester group. The monofunctionalhydrophobic methacrylic acid ester preferably comprises no carboxylgroups, hydroxyl groups, amide groups, sulfonic acid groups, sulfategroups, phosphate groups or phosphonate groups.

The esters preferably are alkyl esters. According to the invention,cycloalkyl esters are also included in alkyl esters. According to apreferred embodiment, the alkyl esters are esters of methacrylic acidand alcohols comprising 1 to 20 carbon atoms, more preferably 1 to 10carbon atoms, even more preferably 1 to 6 carbon atoms, and particularlypreferably 1 to 4 carbon atoms. The alcohols can be substituted ornon-substituted and preferably are non-substituted. Moreover, thealcohols can be saturated or unsaturated and preferably are saturated.

The monomer for radical polymerisation used according to the inventionpreferably has a molar mass of less than 1,000 g/mol. This alsocomprises monomers for radical polymerisation that are components of amixture of monomers, whereby at least one of the monomers for radicalpolymerisation of the mixture of monomers has a defined structure with amolar mass of less than 1,000 g/mol.

The monomer for radical polymerisation is preferably characterised inthat an aqueous solution of the monomer for radical polymerisation has apH in the range of 5 to 9, preferably in the range of 5.5 to 8.5, evenmore preferably in the range of 6 to 8, and particularly preferably inthe range of 6.5 to 7.5.

According to a particularly preferred embodiment, the methacrylatemonomer is a methacrylic acid methylester, methacrylic acid ethylesteror a mixture of said two monomers.

Preferably, the paste according to the invention contains an amount ofthe monomer for radical polymerisation in a range of 15 to 85% byweight, more preferably 20 to 70% by weight, even more preferably 25 to60% by weight, and particularly preferably 25 to 50% by weight, eachrelative to the total weight of the paste according to the invention.

The paste according to the invention contains, as further component, atleast one polymer that is soluble in said at least one monomer forradical polymerisation. According to the invention, a polymer is solublein the polymerisable monomer, if at least 10 g/l, preferably at least 25g/l, more preferably at least 50 g/l, and particularly preferably atleast 100 g/l of the polymer dissolve in said polymerisable monomer. Thepolymer that is soluble in the polymerisable monomer can be ahomopolymer or a copolymer. Said soluble polymer preferably is a polymerwith a mean (by weight) molar mass of at least 150,000 g/mol. Thesoluble polymer can, for example, be a polymer or copolymer of amethacrylic acid ester. According to a particularly preferredembodiment, the at least one soluble polymer is selected from the groupconsisting of polymethacrylic acid methylester (PMMA), polymethacrylicacid ethylester (PMAE), polymethacrylic acid propylester (PMAP),polymethacrylic acid isopropylester,poly(methylmethacrylate-co-methylacrylate),poly(styrene-co-methylmethacrylate), and a mixture of at least two ofsaid polymers.

The amount of the polymer that is soluble in said monomer for radicalpolymerisation that is present in the paste usually is in a range of 1to 85% by weight, relative to the total weight of the paste according tothe invention.

Moreover, the paste according to the invention contains at least onefilling agent that is poorly soluble or insoluble in the at least onemonomer for radical polymerisation, whereby the filling agent is aparticulate inorganic filling agent possessing a BET surface of at least40 m²/g, particularly preferably of at least 200 m²/g, and mostpreferably of at least 300 m²/g.

The BET measurement is an analytical procedure for characterisation ofthe surface of solids by means of gas adsorption. Said determinationmethod is described in DIN ISO 9277:2003-05 (Determination of thespecific surface of solids by gas adsorption according to the BETmethod.

According to a preferred refinement of the paste according to theinvention, the particulate inorganic filling agent is a particulateinorganic filling agent that comprises hydroxy groups that are boundcovalently to the particles. Said hydroxy groups that are arranged onthe surface of the particles allow hydrogen bonds between the fillingagent particles to form, which can be released reversibly through theaction of mechanical or thermal energy. Particulate inorganic fillingagents comprising silanol groups (HO—Si groups) are particularlypreferred.

In this context, according to the invention, it is preferred that theparticulate inorganic filling agent is selected from the groupconsisting of pyrogenic silicon dioxide, pyrogenic metal-silicon mixedoxides, titanium dioxide, bentonite, montmorillonite, and a mixture ofat least two of these substances.

Moreover, it is also feasible to use pyrogenic silicon dioxide madehydrophobic. The hydrophobic silicon dioxide can be produced accordingto the prior art through treating pyrogenic silicon dioxide withdialkyldichlorosilanes (e.g. dimethyldichlorosilane).

Pyrogenic silicon dioxide with a BET surface of at least 40 m²/g,particularly preferably of 200 m²/g, and most preferably of 300 m²/g isparticularly preferred as particulate inorganic filling agent. Saidpyrogenic silicon dioxide is commercially available by the brand name ofAerosil® having specific BET surfaces of 50 m²/g, 90 m²/g, 200 m²/g, and380 m²/g. Mixed oxides of silicon and metal oxides instead of pyrogenicsilicon dioxide are well-suited as well. Mixed oxides of silicon andiron are well-suited as well.

The amount of the particulate inorganic filling agent that is present inthe paste according to the invention usually is in a range of 0.5 to 25%by weight, particularly preferably from 1 to 20% by weight, and mostpreferably in a range of 5 to 15% by weight, each relative to the totalweight of the paste. Aside from the particulate inorganic filling agentdescribed above, the paste according to the invention can containcertain amounts of another filling agent, if applicable, for example thecross-linked polymer particles that are known according to the priorart, whereby the weight ratio of particulate inorganic filling agent tocross-linked polymer particles in this case preferably is at least 1:15(i.e. at least approx. 6% by weight particulate inorganic filling agentrelative to the total amount of filling agent), particularly preferablyis at least 1:1 (i.e. at least 50% by weight particulate inorganicfilling agent relative to the total amount of filling agent).

Preferably, the paste according to the invention is tack-free inaccordance with ISO 5833 no later than 15 minutes after being produced.

Moreover, the paste according to the invention can contain at least onepolymerisation initiator (which preferably is soluble in the monomer forradical polymerisation), at least one polymerisation accelerator (whichpreferably is soluble in the monomer for radical polymerisation), atleast one polymerisation co-accelerator, if applicable, or at least onepolymerisation initiator, at least one polymerisation accelerator, and,if applicable, at least one polymerisation co-accelerator.

In the case of a one-component system, the polymerisation initiatorpreferably is an activatable polymerisation initiator, e.g. aphotoinitiator that is dissolved or suspended in the paste or aphotoinitiator system that is dissolved or suspended in the paste. It isfeasible just as well to provide an initiator or initiators whereit/they are temporarily in contact with the paste, for example in acontainer part, a dosing facility or a transport cannula. Moreover, in aone-component system, the paste according to the invention can alsocontain an electrically conductive radio-opaquer aside from theactivatable polymerisation initiator. Particles made of cobalt, iron,NdFeB, SmCo, cobalt-chromium steel, zirconium, hafnium, titanium,titanium-aluminium-silicon alloys, and titanium-niobium alloys having aparticle size of 0.5-500 μm are particularly well-suited in thiscontext. It is feasible to induce eddy currents in said electricallyconductive radio-opaquer through alternating magnetic fields with afrequency in the range of 500 Hz to 50 kHz which cause the radio-opaquerto heat up. Due to heat transmission, the initiator is heated as welland induced to thermally disintegrate.

In the case of a paste according to the invention that was obtainedthrough combining two pastes of a two-component system, said pastepreferably contains at least one polymerisation initiator (that wascontained in the one paste of the two-component system) and at least onepolymerisation accelerator (that was contained in the other paste of thetwo-component system).

Conceivable as polymerisation initiator are, in particular, peroxidesand barbituric acid derivatives, whereby preferably at least 1 g/l, morepreferably at least 3 g/l, even more preferably at least 5 g/l, andparticularly preferably at least 10 g/l of the peroxides and barbituricacid derivatives can dissolve(s) in the polymerisable monomer at atemperature of 25° C.

According to the invention, a peroxide is understood to mean compoundsthat contain at least one peroxo group (—O—O—). The peroxide preferablycomprises no free acid groups. The peroxide can be an inorganic peroxideor an organic peroxide, such as, for example, a toxicologicallyacceptable hydroperoxide. According to a particularly preferredembodiment, the peroxide is selected from the group consisting ofcumene-hydroperoxide, 1,1,3,3-tetramethylbutyl-hydroperoxide,t-butyl-hydroperoxide, t-amyl-hydroperoxide,di-isopropylbenzen-monohydroperoxide, and a mixture of at least two ofthese substances.

The barbituric acid derivative preferably is a barbituric acidderivative selected from the group consisting of 1-mono-substitutedbarbiturates, 5-mono-substituted barbiturates, 1,5-di-substitutedbarbiturates, and 1,3,5-tri-substituted barbiturates. According to aparticular refinement of the paste according to the invention, thebarbituric acid derivative is selected from the group consisting of1,5-di-substituted barbiturates and 1,3,5-tri-substituted barbiturates.

There is no limitation with regard to the type of substituents on thebarbituric acid. The substituents can, for example, be aliphatic oraromatic substituents. In this context, alkyl, cycloalkyl, allyl or arylsubstituents can be preferred. The substituents can also include heteroatoms. In particular, the substituents can be thiol substituents.Accordingly, 1,5-disubstituted thiobarbiturates or 1,3,5-trisubstitutedthiobarbiturates can be preferred. According to a preferred embodiment,the substituents each have a length of 1 to 10 carbon atoms, morepreferably a length of 1 to 8 carbon atoms, and particularly preferablya length in the range of 2 to 7 carbon atoms. According to theinvention, barbiturates bearing one substituent each at position 1 andposition 5 or a substituent at positions 1, 3, and 5 are preferred.According to another preferred embodiment, the barbituric acidderivative is a 1,5-disubstituted barbiturate or a 1,3,5-trisubstitutedbarbiturate.

According to a particularly preferred embodiment, the barbituric acidderivative is selected from the group consisting of1-cyclohexyl-5-ethyl-barbituric acid, 1-phenyl-5-ethyl-barbituric acid,and 1,3,5-trimethyl-barbituric acid.

Heavy metal compounds selected from the group consisting of heavy metalsalts and heavy metal complexes are preferred as polymerisationaccelerator.

Heavy metal compounds that are preferred according to the invention areselected from the group consisting of copper(II) hydroxide, copper(II)methacrylate, copper(II) acetylacetonate, copper(II)-2-ethyl-hexanoate,cobalt(II) hydroxide, cobalt(II)-2-ethyl-hexanoate, basic copper(II)carbonate, iron(II)-2-ethyl-hexanoate, iron(III)-2-ethyl-hexanoate, anda mixture of at least two of these substances.

According to another refinement of the paste according to the invention,the polymerisation accelerator is selected from the group consisting ofN,N-dimethyl-p-toluidine, N,N-bishydroxyethyl-p-toluidine,N,N-dimethyl-aniline, trioctylmethylammoniumchloride,tetrabutylammoniumchloride, lithium chloride, saccharin,1,8-diazabicyclo[5.4.0]undec-7-ene, and1,5-diazabicyclo(4.3.0)non-5-ene, phthalimide, maleimide, succinimide,pyromellitic acid diimide, and a mixture of at least two of thesesubstances.

Another advantageous refinement of the invention consists of the use, aspolymerisation accelerator, of combinations of heavy metal salts and atleast one member of the group consisting of N,N-dimethyl-p-toluidine,N,N-bis-hydroxyethyl-p-toluidine, N,N-dimethyl-aniline,trioctylmethylammoniumchloride, tetrabutylammoniumchloride, lithiumchloride, saccharin, 1,8-diazabicyclo[5.4.0]undec-7-ene, and1,5-diazabicyclo(4.3.0)non-5-ene, phthalimide, maleimide, succinimide,and pyromellitic acid diimide. Combinations of two and combinations ofthree different polymerisation accelerators in this context are includedin the scope of the invention.

An advantageous refinement of the invention consists of the pasteaccording to the invention containing at least one polymerisationco-accelerator, if applicable, whereby tertiary amines and amidines arepreferred as polymerisation co-accelerators, and wherebyN,N-dimethyl-p-toluidine, N,N-bis-hydroxyethyl-p-toluidine,N,N-dimethyl-aniline, 1,8-diazabicyclo[5.4.0-]undec-7-ene, and1,5-diazabicyclo(4.3.0)-non-5-ene are particularly preferred asco-accelerators.

The paste according to the invention can contain a (total) amount of upto 10% by weight, relative to the total weight of the paste according tothe invention, of the polymerisation initiator, polymerisationaccelerator, polymerisation co-accelerator or polymerisation acceleratorand polymerisation co-accelerator.

The paste according to the invention can contain further ingredientsaside from the components specified above.

According to a preferred embodiment of the paste according to theinvention, said paste can contain at least one radio-opaquer. Theradio-opaquer can be a common radio-opaquer in this field. Suitableradio-opaquers can be soluble or insoluble in the monomer for radicalpolymerisation. The radio-opaquer is preferably selected from the groupconsisting of metal oxides (such as, for example, zirconium oxide),barium sulfate, toxicologically acceptable heavy metal particles (suchas, for example, tantalum), ferrite, magnetite (supramagnetic magnetitealso, if applicable), and biocompatible calcium salts. Saidradio-opaquers preferably have a mean particle diameter in the range of10 nm to 500 μm. Moreover, conceivable radio-opaquers also includeesters of 3,5-bis(acetamido)-2,4,6-triiodobenzoic acid, gadoliniumcompounds, such as gadolinium chelate involving the esters of1,4,7,10-tetraazacyclododecan-1,4,7,10-tetraacetic acid (DOTA). Theconcentration of radiopaquer, in particular the concentration ofzirconium dioxide, that is present in the paste according to theinvention can, for example, be in a range of 3 to 30% by weight.

According to a further preferred embodiment, the paste according to theinvention can contain at least one colourant. The colourant can be acommon colourant in this field and preferably can be a food colourant.Moreover, the colourant can be soluble or insoluble in the at least onemonomer for radical polymerisation. According to a particularlypreferred embodiment, the colourant is selected from the groupconsisting of E101, E104, E132, E141 (chlorophyllin), E142, riboflavin,and lissamine green. According to the invention, the term, colourant,shall also include colour varnishes, such as, for example, colourvarnish green, the aluminium salt of a mixture of E104 and E132.

According to a further preferred embodiment, the paste according to theinvention can contain at least one pharmaceutical agent. The at leastone pharmaceutical agent can be present in the paste according to theinvention in dissolved or suspended form. The pharmaceutical agent canpreferably be selected from the group consisting of antibiotics,antiphlogistic agents, steroids, hormones, growth factors,bisphosphonates, cytostatic agents, and gene vectors. According to aparticularly preferred embodiment, the at least one pharmaceutical agentis an antibiotic. Preferably, the at least one antibiotic is selectedfrom the group consisting of aminoglyoside antibiotics, glycopeptideantibiotics, lincosamide antibiotics, gyrase inhibitors, carbapenems,cyclic lipopeptides, glycylcyclines, oxazolidones, and polypeptideantibiotics. According to a particularly preferred embodiment, the atleast one antibiotic is a member selected from the group consisting ofgentamicin, tobramycin, amikacin, vancomycin, teicoplanin, dalbavancin,lincosamine, clindamycin, moxifloxacin, levofloxacin, ofloxacin,ciprofloxacin, doripenem, meropenem, tigecycline, linezolide,eperezolide, ramoplanin, metronidazole, timidazole, omidazole, andcolistin, as well as salts and esters thereof. Accordingly, the at leastone antibiotic can be selected from the group consisting of gentamicinsulfate, gentamicin hydrochloride, amikacin sulfate, amikacinhydrochloride, tobramycin sulfate, tobramycin hydrochloride, clindamycinhydrochloride, lincosamine hydrochloride, and moxifloxacin. The at leastone antiphlogistic agent is preferably selected from the groupconsisting of non-steroidal antiphlogistic agents and glucocorticoids.According to a particularly preferred embodiment, the at least oneantiphlogistic agent is selected from the group consisting ofacetylsalicylic acid, ibuprofen, diclofenac, ketoprofen, dexamethasone,prednisone, hydrocortisone, hydrocortisone acetate, and fluticasone. Theat least one hormone is preferably selected from the group consisting ofserotonin, somatotropin, testosterone, and estrogen. Preferably, the atleast one growth factor is selected from the group consisting offibroblast growth factor (FGF), transforming growth factor (TGF),platelet derived growth factor (PDGF), epidermal growth factor (EGF),vascular endothelial growth factor (VEGF), insulin-like growth factors(IGF), hepatocyte growth factor (HGF), bone morphogenetic protein (BMP),interleukin-1B, interleukin 8, and nerve growth factor. The at least onecytostatic agent is preferably selected from the group consisting ofalkylating agents, platinum analogues, intercalating agents, mitosisinhibitors, taxanes, topoisomerase inhibitors, and antimetabolites. Theat least one bisphosphonate is preferably selected from the groupconsisting of zoledronate and aledronate.

According to a further preferred embodiment, the paste according to theinvention can contain at least one biocompatible elastomer. Preferably,the biocompatible elastomer is particulate. Preferably, thebiocompatible elastomer is soluble in the at least one monomer forradical polymerisation. The use of butadiene as biocompatible elastomerhas proven to be particularly well-suited.

According to a further preferred embodiment, the paste according to theinvention can contain at least one monomer having adsorption groups. Theadsorption group can, for example, be an amide group. Accordingly, themonomer with adsorption group can, for example, be methacrylic acidamide. Using at least one monomer with adsorption groups would allow thebinding of the bone cement to articular endoprostheses to be influencedin a targeted manner.

According to a further preferred embodiment, the paste according to theinvention can contain at least one stabiliser. The stabiliser should besuitable to prevent spontaneous polymerisation of the monomers forradical polymerisation that are contained in the paste. Moreover, thestabiliser should not undergo interfering interactions with the otheringredients contained in the paste according to the invention.Stabilisers of said type are known according to the prior art. Accordingto a preferred embodiment, the stabiliser is2,6-di-tert-butyl-4-methylphenol and/or 2,6-di-tertbutyl-phenol.

A kit comprising a paste A and a paste B also makes a contribution to asolution meeting the object specified above,

whereby(a) paste A contains

-   -   (a1) at least one monomer for radical polymerisation;    -   (a2) at least one polymer that is soluble in (a1); and    -   (a3) at least one polymerisation initiator;        (b) paste B contains    -   (b1) at least one monomer for radical polymerisation;    -   (b2) at least one polymer that is soluble in (b1); and    -   (b3) at least one polymerisation accelerator;        and whereby at least one of the pastes A and B contains as        component (a4) and/or (b4) at least one filling agent that is        poorly soluble or insoluble in (a1)) and/or (b1), respectively,        whereby the filling agent is a particulate inorganic filling        agent possessing a BET surface of at least 40 m²/g, particularly        preferably of at least 200 m²/g, and most preferably of at least        300 m²/g.

According to the invention, a kit shall be understood to be a systemmade up of at least two components. Although reference to two components(i.e. paste A and paste B) is made in the following, the kit can just aswell contain more than two components, for example three, four, five ormore than five components, according to need. The individual componentspreferably are provided to be packaged separate from each other suchthat the ingredients of the one kit component do not contact theingredients of another kit component. Accordingly, it is feasible, forexample, to package the respective kit components separate from eachother and to store them together in a reservoir container.

Preferably, the kit is designed as a kit for producing bone cementcomprising a first container and a second container, whereby the firstcontainer comprises paste A and the second container comprises paste B,whereby at least one of the containers can be opened to allow for pasteA and paste B to be mixed after the opening, and a mixing unit for themixing of pastes A and B.

The components described above in the context of the paste according tothe invention as preferred monomer for radical polymerisation, aspolymer that is soluble in said monomer, as polymerisation initiator, aspolymerisation accelerator, and as particulate inorganic filling agentare preferred as monomer (a1)) and/or (b1) for radical polymerisation,as polymer that is soluble in (a1)) and/or (b1), as polymerisationinitiator (a3), as polymerisation accelerator (b3), and as particulateinorganic filling agent (a4) and/or (b4), respectively.

Preferably, paste A and paste B contain an amount of the at least onemonomer for radical polymerisation (a1) and/or (b1) in a range of 15 to85% by weight, more preferably 20 to 70% by weight, even more preferably25 to 60% by weight, and particularly preferably 25 to 50% by weight,each relative to the total weight of paste A and/or paste B.

Preferably, paste A contains an amount of the polymerisation initiator(a3) in a range of 0.01 to 10% by weight, more preferably in a range of0.01 to 8% by weight, and even more preferably in a range of 0.01 to 5%by weight, each relative to the total weight of paste A.

Provided the polymerisation accelerator (b3) is a heavy metal compoundselected from the group consisting of heavy metal salts and heavy metalcomplexes, in particular is a heavy metal compound selected from thegroup consisting of copper(II) hydroxide, copper(II) methacrylate,copper(II) acetylacetonate, copper(II)-2-ethyl-hexanoate, cobalt(II)hydroxide, cobalt(II)-2-ethyl-hexanoate, basic copper(II) carbonate,iron(II)-2-ethyl-hexanoate, iron(III)-2-ethyl-hexanoate, and a mixtureof at least two of these substances, paste B preferably contains anamount of said polymerisation accelerator (b3) in a range of 0.0005 to0.5% by weight, relative to the total weight of paste B.

Provided the polymerisation accelerator (b3) is a compound selected fromthe group consisting of N,N-dimethyl-p-toluidine,N,N-bis-hydroxyethyl-p-toluidine, N,N-dimethyl-aniline,trioctylmethylammoniumchloride, tetrabutylammoniumchloride, lithiumchloride, saccharin, 1,8-diazabicyclo[5.4.0]undec-7-ene,1,5-diazabicyclo(4.3.0)non-5-ene, phthalimide, maleimide, succinimide,pyromellitic acid diimide, and a mixture of at least two of thesesubstances, paste B preferably contains an amount of said polymerisationaccelerator (b3) in a range of 0.1 to 10% by weight, relative to thetotal weight of paste B.

Specifically, paste A can further contain as component (a5) thepolymerisation co-accelerator described above, which preferably is acompound selected from the group consisting of N,N-dimethyl-p-toluidine,N,N-bis-hydroxyethyl-p-toluidine, N,N-dimethyl-aniline,1,8-diazabicyclo[5.4.0]undec-7-ene, 1,5-diazabicyclo(4.3.0)non-5-ene,and a mixture of at least two of these substances. It is preferred inthis context for paste A to contain an amount of the at least onepolymerisation co-accelerator (a5) in a range of 0.1 to 10% by weight,relative to the total weight of paste A.

Provided one of the pastes of the kit according to the inventioncontains the poorly soluble or insoluble filling agent and the otherpaste contains no poorly soluble or insoluble filling agent at all orcontains a negligible amount of poorly soluble or insoluble fillingagent as compared to the amount present in the other paste, the kit iscalled “asymmetrical”. In contrast, a so-called “symmetrical” kit hasapproximately comparable amounts of the poorly soluble or insolublefilling agent present in both pastes.

Moreover, pastes A and/or B can contain further additives aside from thecomponents described above, such as radio-opaquers, colourants,pharmaceutical agents, biocompatible elastomers, monomers havingadhesion groups or stabilisers, whereby the components described above,in the context of the paste according to the invention, as preferredradio-opaquers, colourants, pharmaceutical agents, biocompatibleelastomers, monomers having adhesion groups, and stabilisers arepreferred here as well.

According to a first particular refinement of the kit according to theinvention, the kit is an “asymmetrical” kit. It is preferred in thiscontext for paste A to contain 1 to 50% by weight, particularlypreferably 1.0 to 15% by weight, even more preferably 30 to 55% byweight, and most preferably 1 to 5% by weight, each relative to thetotal weight of paste A, of the filling agent (a4) that is insoluble in(a1), and for paste B to contain less than 5% by weight, particularlypreferably less than 1% by weight, even more preferably less than 0.1%by weight, and yet more preferably less than 0.01% by weight, eachrelative to the total weight of paste B, of the filling agent (b4) thatis insoluble in (b1), whereby it is most preferred for paste B tocontain no filling agent (b4) that is insoluble in (b1) at all.

Moreover, in the context of said first particular refinement of the kitaccording to the invention, it is preferred for paste A to contain anamount of the polymer (a2) that is soluble in (a1) in a range of 1 to25% by weight, particularly preferably in a range of 2 to 20% by weight,even more preferably in a range of 2 to 18% by weight, and mostpreferably in a range of 3 to 16% by weight, each relative to the totalweight of paste A, and for paste B to contain an amount of a polymer(b2) that is soluble in (b1) in a range of 25 to 85% by weight,particularly preferably in a range of 35 to 85% by weight, even morepreferably in a range of 35 to 80% by weight, and most preferably in arange of 35 to 75% by weight, each relative to the total weight of pasteB.

Moreover, it is preferred in the context of said first particularrefinement of the kit according to the invention that the weight ratioof filling agent (b4) that is insoluble in (b1) to the at least onepolymer (b2) that is soluble in (b1) is no more than 0.2, morepreferably no more than 0.15, even more preferably no more than 0.1, yetmore preferably no more than 0.05, particularly preferably no more than0.02, and even more particularly preferably is equal to 0.

According to a second particular refinement of the kit according to theinvention, the kit is a “symmetrical” kit. It is preferred in thiscontext for paste A to contain 0.5 to 35% by weight, particularlypreferably 0.5 to 15% by weight, and even more preferably 20 to 75% byweight, each relative to the total weight of paste A, of the fillingagent (a4) that is insoluble in (a1), and for paste B to contain 0.5 to35% by weight, particularly preferably 0.5 to 15% by weight, and evenmore preferably 0.5 to 5% by weight, each relative to the total weightof paste B, of the filling agent (b4) that is insoluble in (b1).

Moreover, in the context of said second particular refinement of the kitaccording to the invention, it is preferred that paste A contains anamount of a polymer (a2) that is soluble in (a1) in a range of 5 to 50%by weight, particularly preferably in a range of 10 to 40% by weight,and even more preferably in a range of 20 to 30% by weight, eachrelative to the total weight of paste A, and/or paste B contains anamount of a polymer (b2) that is soluble in (b1) in a range of 5 to 50%by weight, particularly preferably in a range of 10 to 40% by weight,and even more preferably in a range of 20 to 30% by weight, eachrelative to the total weight of paste B.

According to the invention, the purpose of the paste and/or kitaccording to the invention containing at least pastes A and B is theproduction of bone cement.

Referring to the kit, for this purpose, the at least two pastes A and Bare mixed with each other, upon which another paste, paste C, isobtained. The mixing ratio preferably is 0.5 to 1.5 parts by weight ofpaste A and 0.5 to 1.5 parts by weight of paste B. According to aparticularly preferred embodiment, the fraction of paste A is 30 to 70%by weight and the fraction of paste B is 30 to 70% by weight, eachrelative to the total weight of pastes A and B, respectively. Mixing canbe effected with common mixing devices, for example a static mixer or adynamic mixer.

After mixing the pastes of the kit, paste C which is ultimately obtained(and corresponds to the paste according to the invention specifiedabove) is tack-free in accordance with the ISO 5833 standard no laterthan after 15 minutes.

The bone cement generated from paste C by curing attains high strengthapproximately six to eight minutes after mixing the pastes contained inthe kit.

According to a preferred embodiment, paste C and/or the kit according tothe invention can be used for mechanical fixation of articularendoprostheses, for covering skull defects, for filling bone cavities,for femuroplasty, for vertebroplasty, for kyphoplasty, for themanufacture of spacers, and for the production of carrier materials forlocal antibiotics therapy.

In this context, the term, “spacer”, shall be understood to meanimplants that can be used temporarily as spacer in the scope of thetwo-step exchange of prostheses in septic revision surgeries.

Carrier materials for local antibiotics therapy can be provided asspheres or sphere-like bodies or as bean-shaped bodies. Besides, it isalso feasible to produce rod-shaped or disc-shaped carrier materialsthat conatin the bone cement made from the paste according to theinvention and/or the kit according to the invention. Moreover, thecarrier materials can also be threaded onto absorbable or non-absorbablesuture material in a bead-like manner.

The uses according to the invention of bone cement described above areknown from the literature and have been described therein on numerousoccasions.

A contribution to meeting the objects specified above is also made by aform body that is obtainable through polymerisation of a paste that isobtainable through mixing paste A and paste B of the kit according tothe invention or through polymerisation of a paste according to theinvention. Form bodies according to the scope of the present inventioncan be any three-dimensional bodies, in particular the “spacers”described above.

The invention shall be illustrated through the examples described in thefollowing, though without limiting the scope of the invention.

EXEMPLARY EMBODIMENTS

Pastes A of examples A1-6 were produced by simply mixing the components.The pastes thus formed were then stored over night at room temperature.

Paste A

Compositions of pastes A Example CH BH DM EG MA MMA PL1 AE ZrO₂ Rod no.[mg] [g] [g] [g] [g] [g] [g] [g] [g] [mg] A1 75 2.00 — — — 14.00 6.002.00 20.00 20 A2 50 1.80 0.20 — — 14.00 7.00 1.50 20.00 20 A3 50 1.800.20 0.50 — 13.50 7.00 1.00 20.00 20 A4 50 1.90 0.10 — — 14.00 6.00 1.5020.00 20 A5 50 1.40 0.60 0.10 0.40 17.70 13.60 1.00 4.80 20 A6 50 1.400.60 0.10 0.40 17.70 13.60 2.00 4.80 20 CH: Cumene hydroperoxide BH:N,N-Bis-(2-hydroxyethyl)-p-toluidine DM: N,N-Dimethyl-p-toluidine EG:Ethylene glycol dimethacrylate MA: Methacrylamide MMA:Methylmethacrylate PL1: linearpoly(methylmethacrylate-co-methylacrylate) MW <500,000 g/mol AE:Aerosil ® 380 (pyrogenic silicic acid) ZrO₂: Zirconium dioxide Rod:2,6-Di-t-butyl-4-methyl-phenol

Pastes B of examples B1-6 were produced by simply mixing the components.The pastes thus formed were then stored over night at room temperature.

Paste B

Compositions of pastes B Example SAC CuOct MMA PL1 AE Rod no. [g] [mg][g] [g] [g] [mg] B1 1.00 55 22.00 18.00 — 35 B2 1.00 55 23.00 17.00 — 35B3 1.00 55 23.00 17.00 — 35 B4 1.00 55 22.00 18.00 0.50 35 B5 1.00 5521.20 17.50 — 35 B6 1.00 55 21.20 17.50 — 35 SAC: Saccharine CuOct:Copper(II)-2-ethylhexanoate MMA: Methylmethacrylate PL1: linearpoly(methylmethacrylate-co-methylacrylate), MW <500,000 g/mol AE:Aerosil ® 380 (pyrogenic silicic acid) Rod:2,6-Di-t-butyl-4-methyl-phenol

The pastes A and B of examples A1-6 and B1-6 were mixed with each otherat a weight ratio of 1:1. This produced pastes C that were tack-freeright away and, in the case of pastes C1 to C4, had a processing time ofup to 20 minutes. During the processing phase, it was feasible to forcesaid pastes through 18 G cannulas (cannula with an external diameter of1.2 mm) without any difficulty.

In contrast, the viscosity and the processing phase of pastes C5 and C6were similar to conventional high viscosity polymethylmethacrylate bonecements. The processing phase lasted for 4-5 minutes.

The mixed pastes C produced from pastes A and B of examples 1-6 (weightratio of paste A to paste B of 1:1) were used to produce strip-shapedtest bodies with dimensions of (75 mm×10 mm×3.3 mm) for the assay ofbending strength and flexural modulus and cylindrical test bodies(diameter 6 mm, height 12 mm) were used for the assay of compressivestrength. The test bodies were then stored for 24 hours on air at 23±1°C. Then the 4-point flexural strength, flexural modulus, and thecompressive strength of the test bodies were determined using a Zwickuniversal testing device.

Compositions 4-point flexural Flexural Compressive of strength modulusstrength Pastes C Pastes C [MPa] [MPa] [MPa] C1 A1 + B1 57.9 ± 0.7 2686± 51 102.0 ± 2.4  C2 A2 + B2 58.9 ± 0.4 2643 ± 53 96.5 ± 4.1 C3 A3 + B358.7 ± 1.9  2682 ± 153 94.4 ± 4.3 C4 A4 + B4 62.9 ± 1.7 2927 ± 91 92.2 ±6.2 C5 A5 + B5 58.1 ± 1.4 2405 ± 77 91.2 ± 4.4 C6 A6 + B6 60.1 ± 3.1 2561 ± 192 93.9 ± 3.3

The results of the 4-point flexural strength, flexural modulus, andcompressive strength tests on cured pastes C1-6 show that the mechanicalstability requirements of ISO 5833 are met. ISO 5833 defines thefollowing parameters: 4-point flexural strength of at least 50 MPa,flexural modulus of at least 1,800 MPa, and compressive strength of atleast 70 MPa.

Moreover, additional pastes B that were produced analogous to paste B6except that each had 1.0 g vancomycin hydrochloride, clindamycinhydrochloride, daptomycin, and octenidine dihydrochloride, andgentamicin sulfate added. After mixing these pastes B with paste A1 at aweight ratio of 1:1, the mixed pastes C showed a similar curingbehaviour as the combination of paste A6 and paste B6 at a weight ratioof 1:1.

In addition, pastes were produced using barium sulfate instead ofzirconium dioxide. Said pastes had a similar curing behaviour as thepastes C1-6 produced from pastes A1-6 and B1-6.

Furthermore, pastes A were produced analogous to example A1, but usingt-butyl-hydroperoxid, t-amyl-hydroperoxide, and dicumyl-peroxide insteadof cumene-hydroperoxide. After mixing these pastes A with paste B1 at aweight ratio of 1:1, the mixed pastes showed a similar behaviour as thecombination of pastes A1 and paste B1.

1. Paste containing at least one monomer for radical polymerization, atleast one polymer that is soluble in said at least one monomer forradical polymerization, and at least one filling agent that is poorlysoluble or insoluble in said at least one monomer for radicalpolymerization, wherein the filling agent is a particulate inorganicfilling agent possessing a BET surface of at least 40 m²/g.
 2. Pasteaccording to claim 1, whereby the particulate inorganic filling agentcomprises hydroxy groups that are bound covalently to the particles. 3.Paste according to claim 2, wherein the particulate inorganic fillingagent comprises Ho—Si groups (silanol groups) that are bound covalentlyto the particles.
 4. Paste according to claim 1, wherein the particulateinorganic filling agent is selected from the group consisting ofpyrogenic silicon dioxide, pyrogenic silicon dioxide made hydrophobic,pyrogenic metal-silicon mixed oxides, titanium dioxide, bentonite,montmorillonite, and a mixture of at least two of these substances. 5.Paste according to claim 4, wherein the particulate inorganic fillingagent is pyrogenic silicon dioxide with a BET surface of at least 200m²/g.
 6. Paste according to claim 5, wherein the particulate inorganicfilling agent is pyrogenic silicon dioxide with a BET surface of atleast 300 m²/g.
 7. Paste according to claim 1, wherein the pastecontains 0.5 to 25% by weight, relative to the total weight of thepaste, of the particulate inorganic filling agent.
 8. Paste according toclaim 1, wherein the monomer for radical polymerization is a methacrylicacid ester.
 9. Paste according to claim 1, wherein the paste contains,in addition, at least one polymerization initiator, at least onepolymerization accelerator, at least one polymerization co-accelerator,if applicable, or at least one polymerization initiator, at least onepolymeriation accelerator, and, if applicable, at least onepolymerization co-accelerator.
 10. Paste according to claim 1, whereinthe soluble polymer is selected from the group consisting ofpoly(methacrylic acid methylester), poly(methacrylic acid ethylester),poly(methylmethacrylic acid propylester), poly(methacrylic acidisopropylester), poly(methylmethacrylate-co-methylacrylate),poly(styrene-co-methylmethacrylate), and a mixture of at least two ofsaid polymers.
 11. Paste according to claim 1, wherein the paste istack-free in accordance with ISO 5833 no later than 15 minutes afterbeing produced.
 12. Kit comprising a paste A and a paste B, wherein (a)paste A contains (a1)) at least one monomer for radical polymerization;(a2) at least one polymer that is soluble in (a 1); and (a3) at leastone polymerization initiator; (b) paste B contains (b1) at least onemonomer for radical polymerization; (b2) at least one polymer that issoluble in (b1); and (b3) at least one polymerization accelerator; andwherein at least one of the pastes A and B contains, as component (a4)and/or (b4), respectively, at least one filling agent that is poorlysoluble or insoluble in (a1)) and/or (b1), respectively.
 13. Kitaccording to claim 12, wherein the monomer (a1) and/or (b1) for radicalpolymerization is a methacrylic acid ester.
 14. Kit according to claim12, wherein the at least one polymerization initiator (a3) is selectedfrom the group consisting of barbiturates and peroxides.
 15. Kitaccording to claim 14, wherein the at least one polymerization initiator(a3) is selected from the group consisting of cumene-hydroperoxide,1,1,3,3-tetramethylbutyl-hydroperoxide, t-butyl-hydroperoxide,t-amyl-hydroperoxide, di-isopropylbenzen-monohydroperoxide, and amixture of at least two of these substances.
 16. Kit according to claim12, wherein paste A contains an amount of the at least onepolymerization initiator (a3) in a range of 0.01 to 10% by weight,relative to the total weight of paste A.
 17. Kit according to claim 12,wherein the at least one polymerization accelerator (b3) is at least oneheavy metal compound selected from the group consisting of heavy metalsalts and heavy metal complexes.
 18. Kit according to claim 17, whereinthe heavy metal compound is selected from the group consisting ofcopper(II) hydroxide, copper(II) methacrylate, copper(II)acetylacetonate, copper(II)-2-ethyl-hexanoate, cobalt(II) hydroxide,cobalt(II)-2-ethyl-hexanoate, basic copper(II) carbonate,iron(II)-2-ethyl-hexanoate, iron(III)-2-ethyl-hexanoate, and mixtures ofat least two of these substances.
 19. Kit according to claim 17, whereinpaste B contains an amount of the polymerization accelerator (b3) in arange of 0.0005 to 0.5% by weight, relative to the total weight of pasteB.
 20. Kit according to claim 12, wherein the at least onepolymerization accelerator (b3) is selected from the group consisting ofN,N-dimethyl-p-toluidine, N,N-bis-hydroxyethyl-p-toluidine,N,N-dimethyl-aniline, trioctylmethylammoniumchloride,tetrabutylammoniumchloride, lithium chloride, saccharin,1,8-diazabicyclo[5.4.0]undec-7-ene, and1,5-diazabicyclo(4.3.0)non-5-ene, phthalimide, maleimide, succinimide,pyromellitic acid diimide, and mixtures of at least two of thesesubstances.
 21. Kit according to claim 20, wherein paste B contains anamount of the polymerization accelerator (b3) in a range of 0.1 to 10%by weight, relative to the total weight of paste B.
 22. Kit according toclaim 12, wherein paste B contains, as polymerization accelerator (b3),combinations of heavy metal salts and at least one member selected fromthe group consisting of N,N-dimethyl-p-toluidine,N,N-bis-hydroxyethyl-p-toluidine, N,N-dimethyl-aniline,trioctylmethylammoniumchloride, tetrabutylammoniumchloride, lithiumchloride, saccharin, 1,8-diazabicyclo[5.4.0]undec-7-ene, and1,5-diazabicyclo(4.3.0)non-5-ene, phthalimide, maleimide, succinimide,and pyromellitic acid diimide.
 23. Kit according to claim 12, whereinpaste A contains at least one polymerization co-accelerator (a5)selected from the group consisting of N,N-dimethyl-p-toluidine,N,N-bishydroxyethyl-p-toluidine, N,N-dimethyl-aniline,1,8-diazabicyclo[5.4.0]undec-7-ene, 1,5-diazabicyclo(4.3.0)non-5-ene,and mixtures of at least two of these substances.
 24. Kit according toclaim 23, whereby paste A contains an amount of the at least onepolymerization co-accelerator (a5) in a range of 0.1 to 10% by weight,relative to the total weight of paste A.
 25. Kit according to claim 12,wherein paste A and paste B contain an amount of the at least onemonomer (a1) and/or (b1) for radical polymerization in a range of 15 to85% by weight, each relative to the total weight of paste A and/or pasteB, respectively.
 26. Kit according to claim 12, wherein the polymer (a3)and/or (b3) that is soluble in (a1) and/or (b1), respectively, isselected from the group consisting of poly(methacrylic acidmethylester), poly(methacrylic acid ethylester), poly(methylmethacrylicacid propylester), poly(methacrylic acid isopropylester),poly(methylmethacrylate-co-methylacrylate),poly(styrene-co-methylmethacrylate), and mixtures of at least two ofsaid polymers.
 27. Kit according to claim 12, wherein paste A contains 1to 50% by weight, relative to the total weight of paste A, of fillingagent (a4), and paste B contains less than 5% by weight, relative to thetotal weight of paste B, of a filling agent (b4).
 28. Kit according toclaim 27, wherein paste A contains an amount of the polymer (a2) that issoluble in (a1) in a range of 1 to 25% by weight, relative to the totalweight of paste A, and paste B contains an amount of the polymer (b2)that is soluble in (b1) in a range of 25 to 85% by weight, relative tothe total weight of paste B.
 29. Kit according to claim 12, wherebypaste A contains 0.5 to 35% by weight, relative to the total weight ofpaste A, of filling agent (a4), and paste B contains 0.5 to 35% byweight, relative to the total weight of paste B, of filling agent (b4).30. Kit according to claim 29, wherein paste A contains an amount of thepolymer (a2) that is soluble in (a1) in a range of 5 to 50% by weight,relative to the total weight of paste A, and/or paste B contains anamount of the polymer (b2) that is soluble in (b1) in a range of 5 to50% by weight, relative to the total weight of paste B.
 31. Kitaccording to claim 12, wherein pastes A and/or B contain a sufficientamount of the filling agent (a4) and/or (b4) so that the paste Cproduced through mixing pastes A and B contains an amount of the fillingagent in a range of 0.5 to 25.0% by weight.
 32. A method for mechanicalfixation of articular endoprostheses, for covering skull defects, forfilling bone cavities, for femuroplasty, for vertebroplasty, forkyphoplasty, for the manufacture of spacers or for the production ofcarrier materials for local antibiotics therapy by application of apaste of claim
 1. 33. Form body obtained through polymerization of apaste of claim
 1. 34. Form body obtained through polymerization of apaste produced from the kit of claim 12.